BENITIONSClinical Trial Intelligence

A Study to Evaluate the Safety, Reactogenicity, and Effectiveness of mRNA-1273 Vaccine in Adolescents 12 to <18 Years Old to Prevent COVID-19

第2/3相 完了 NCT04649151

対象疾患SARS-CoV-2
第2/3相
スポンサーModernaTX, Inc.
ステータス完了
参加者数4,328 名
介入(薬剤)mRNA-1273, mRNA-1273.222
開始日2020年12月9日
完了日2024年6月14日
結果公開日2025年9月15日

概要

The mRNA-1273 vaccine is being developed to prevent COVID-19, the disease resulting from Severe Acute Respiratory Syndrome coronavirus (SARS-CoV-2) infection. The study is designed to primarily evaluate the safety, reactogenicity, and effectiveness of mRNA-1273 vaccine administered as primary series and a booster dose (BD) to an adolescent population. The study will also evaluate the safety and immunogenicity of an mRNA-1273.222 vaccine against the SARS-CoV- 2 omicron variant as a primary series.

Number of Participants With Solicited Local and Systemic Adverse Reactions (ARs)

7 days post-vaccination · Participants

Part 1A: mRNA-1273 100 μg586 Participants
Part 1A: Placebo585 Participants
Part 1C-1: mRNA-1273 50 µg BD627 Participants
Part 1C-2: mRNA-1273 50 μg BD42 Participants
Part 2: mRNA-1273 50 μg First Injection25 Participants
Part 2: mRNA-1273 50 μg Second Injection18 Participants

Number of Participants With Unsolicited AEs

Up to 28 days post-vaccination · Participants

Part 1A: mRNA-1273 100 μg582 Participants
Part 1A: Placebo237 Participants
Part 1C-1: mRNA-1273 50 µg BD209 Participants
Part 1C-2: mRNA-1273 50 μg BD19 Participants
Part 2: mRNA-1273 50 μg10 Participants
Part 2: mRNA-1273 50 μg BD2 Participants

Part 1A Geometric Mean Value of Serum Pseudovirus Neutralizing Antibody (nAb) ID50 Titers From Study P203 Vaccine Recipients at Day 57 Compared With Those From Young Adult (18 to 25 Years of Age) Vaccine Recipients (Day 57) in Study P301

Day 57 Study P203/Day 57 Study P301 · titer

Part 1A: mRNA-1273 100 μg1401.670 titer
Study mRNA-1273-P301 (NCT04470427 ) mRNA-1273 100 μg1299.855 titer
GMR1.078 (95% CI 0.940–1.237)

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